EP1749808A1 - Method for the preparation of linear alpha-olefins and reactor system therefore with improved disposal of high molecular weight oligomers - Google Patents
Method for the preparation of linear alpha-olefins and reactor system therefore with improved disposal of high molecular weight oligomers Download PDFInfo
- Publication number
- EP1749808A1 EP1749808A1 EP05016524A EP05016524A EP1749808A1 EP 1749808 A1 EP1749808 A1 EP 1749808A1 EP 05016524 A EP05016524 A EP 05016524A EP 05016524 A EP05016524 A EP 05016524A EP 1749808 A1 EP1749808 A1 EP 1749808A1
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- EP
- European Patent Office
- Prior art keywords
- molecular weight
- high molecular
- weight oligomers
- reactor
- olefins
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- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/02—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons
- C07C2/04—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation
- C07C2/06—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation of alkenes, i.e. acyclic hydrocarbons having only one carbon-to-carbon double bond
- C07C2/08—Catalytic processes
- C07C2/26—Catalytic processes with hydrides or organic compounds
- C07C2/30—Catalytic processes with hydrides or organic compounds containing metal-to-carbon bond; Metal hydrides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/02—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons
- C07C2/04—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation
- C07C2/06—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation of alkenes, i.e. acyclic hydrocarbons having only one carbon-to-carbon double bond
- C07C2/08—Catalytic processes
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S585/00—Chemistry of hydrocarbon compounds
- Y10S585/8995—Catalyst and recycle considerations
- Y10S585/901—Catalyst and recycle considerations with recycle, rehabilitation, or preservation of solvent, diluent, or mass action agent
Definitions
- the present invention relates to a method for the preparation of linear alpha-olefins by oligomerization of ethylene in a reactor in the presence of a solvent and a catalyst.
- Oligomerization methods for preparing linear alpha-olefins are widely known in the art. This method is usually carried out in the presence of a catalyst preferably comprising a zirconium component, such as zirconium tetraisobutyrate, and an aluminum component as activator, such as ethyl aluminum sesquichloride.
- a catalyst preferably comprising a zirconium component, such as zirconium tetraisobutyrate, and an aluminum component as activator, such as ethyl aluminum sesquichloride.
- One problem associated with such oligomerization methods is that not only liquid linear alpha-olefins with desired chain length, e.g. C 4 -C 18 , are prepared, but also high molecular weight oligomers which are solid at reaction temperature of about 60-100°C and have to be removed from the plant to avoid plugging. Such high molecular weight oligomers may be separated from the desired alpha-olefin products.
- a further problem is the disposal of high molecular weight oligomers from the plant, as the amount of high molecular weight oligomers produced is low (some kg/h) and it is often required to transfer the high molecular weight oligomers over a large distance to a disposal device.
- plugging may occur in the piping connecting the reactor unit and the disposal device, such as an incinerator, as well as in any equipment and piping which are in contact with high molecular weight oligomers containing streams. This plugging may also occur due to the low flow rates in the reactor system.
- the distance between the oligomerization reactor and the disposal device is large, for example, about 1 to about 2 kilometers.
- small amounts of high molecular weight oligomers in the range of some kilogram/h are difficult to transfer to the disposal device due to long residence time, and this often results in plugging of equipment and piping.
- a discharge stream of the reactor comprising the solvent, catalyst, linear alpha-olefins and substantially high molecular weight oligomers, the high molecular weight oligomers are separated, then diluted with a dilution medium and heated to about 130°C to about 200°C, the diluted high molecular weight oligomers being then transferred to a disposal device, wherein recycles for loop operation are established, and flow rates of the loop streams are from about 1 to about 50 m 3 /h.
- the high molecular weight oligomers are separated in a separation unit, preferably a filter unit or a distillation unit.
- the temperature in the reactor is from about 60 to about 100°C.
- the solvent may be toluene and the dilution medium may be toluene and/or a liquid fraction of the oligomerization product comprising oligomers having more than 18 carbon atoms.
- the dilution medium comprises the bottom product of a purification apparatus, preferably a distillation column, for the solvent.
- the dilution medium may comprise high molecular weight oligomers.
- the method is further characterized in that the dilution medium with dissolved high molecular weight oligomers is recycled in a loop to increase flow rates from kg/h to m 3 /h with corresponding stream velocities to avoid plugging of lines.
- the disposal device is an incinerator.
- the dilution ratio of the dilution medium: high molecular weight oligomer may be about 5:1 to about 15:1, preferably about 10:1.
- a reactor system for preparing linear alpha-olefins comprising a reactor, a separation unit for separating high molecular weight oligomers, recycle loops, and a transfer line to a disposal device.
- inventive method is not necessarily restricted to the oligomerization of ethylene to obtain linear alpha-olefins, but may be utilized in all technologies handling high molecular weight oligomers.
- a reactor 1 for the oligomerization of ethylene to prepare linear alpha-olefins is provided.
- ethylene is oligomerized in the presence of a solvent and a catalyst, preferably at a temperature of about 60-100°C.
- a discharge stream is removed from the reactor via a discharge line 2.
- the discharge stream comprises the solvent, catalyst, liquid linear alpha-olefins and high molecular weight oligomers.
- high molecular weight oligomers is meant to comprise oligomers having such a high molecular weight that they are substantially solid at reaction temperature.
- the discharge stream may be transferred via the discharge line 2 to a separation unit 3, also held at a temperature of about 60-100°C, wherein solid high molecular weight oligomers are separated from the liquid discharge stream.
- the separation unit may be a filter or any other means suitable and known for someone skilled in the art. Such a separation unit is not absolutely necessary, for example, if no high molecular weight oligomers being solid at reaction temperature are present.
- the discharge stream containing the substantial amount of solvent and liquid linear alpha-olefins may be processed as is known for someone skilled in the art, for example by distillation of the respective linear alpha-olefins.
- the solvent utilized for the oligomerization process is preferably toluene.
- Toluene is provided to and removed from the reactor by a reactor flushing system 4.
- the reactor flushing system 4 is further connected to a solvent purification apparatus 5, preferably a distillation equipment.
- the solvent may be purified and purified solvent may be reintroduced into the reactor 1.
- Impurities which may be incorporated in the solvent may be also high molecular weight oligomers which are collected in the bottoms product of the solvent purification apparatus 5.
- the bottom product may be used as dilution medium.
- the bottom product comprising also high molecular weight oligomers is removed from the solvent purification apparatus 5 via line 7.
- Lines 6 and 7 are combined.
- the combined streams are then heated to a temperature of about 130°C to about 200°C so that the high molecular weight oligomers may be diluted or melted (as polyethylene being a major component of the high molecular weight oligomers has a melting point of about 130°C).
- the weight ratio of high molecular weight oligomers and dilution medium is from about 1:5 to about 1:15, preferably 1:10.
- the high molecular weight oligomers containing streams are also agitated.
- the combined streams may be then transferred via line 8 to a tank 9 where the combined streams may be additionally diluted with further dilution medium. Also, fractions of the linear alpha-olefins having more than 18 carbon atoms may be added at this stage, or even earlier or later. As it is still difficult to find economically attractive applications for the fractions of C 20+ these fractions may be preferably utilized to dilute the high molecular weight oligomers for disposal. From the tank 9 the diluted high molecular weight oligomers may be then transferred via line 10 to a disposal device, preferably an incinerator 11. From line 10 the diluted high molecular weight oligomers may be also recycled via recycle line 12 into tank 9. The effluent of tank 9 may be also recycled via recycle line 13 to lines 6 and 7.
- high molecular weight oligomers containing streams are diluted with an appropriate dilution medium, kept at elevated temperature and, optionally, agitated.
- stream velocities in the equipment and piping may be kept high by establishing of larger pump flow rates which are in the range of about 1 to about 50 m 3 /h. Due to the high stream velocities any plugging of equipment and piping may be avoided. Additionally, the viscosity and pressure drop of the piping system can be adjusted by the dilution rate of the high molecular weight oligomers in the dilution medium.
- the small amounts of high molecular weight oligomers (in the range of some kg/h) obtained in the inventive method may be easily disposed by dilution and heating with prevention of plugging.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polymerisation Methods In General (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Description
- The present invention relates to a method for the preparation of linear alpha-olefins by oligomerization of ethylene in a reactor in the presence of a solvent and a catalyst.
- Oligomerization methods for preparing linear alpha-olefins are widely known in the art. This method is usually carried out in the presence of a catalyst preferably comprising a zirconium component, such as zirconium tetraisobutyrate, and an aluminum component as activator, such as ethyl aluminum sesquichloride.
- One problem associated with such oligomerization methods is that not only liquid linear alpha-olefins with desired chain length, e.g. C4-C18, are prepared, but also high molecular weight oligomers which are solid at reaction temperature of about 60-100°C and have to be removed from the plant to avoid plugging. Such high molecular weight oligomers may be separated from the desired alpha-olefin products. A further problem is the disposal of high molecular weight oligomers from the plant, as the amount of high molecular weight oligomers produced is low (some kg/h) and it is often required to transfer the high molecular weight oligomers over a large distance to a disposal device. In the piping connecting the reactor unit and the disposal device, such as an incinerator, as well as in any equipment and piping which are in contact with high molecular weight oligomers containing streams, plugging may occur. This plugging may also occur due to the low flow rates in the reactor system.
- In some cases, the distance between the oligomerization reactor and the disposal device is large, for example, about 1 to about 2 kilometers. Thus, small amounts of high molecular weight oligomers (in the range of some kilogram/h) are difficult to transfer to the disposal device due to long residence time, and this often results in plugging of equipment and piping.
- It is therefore an object of the present invention to provide a method for the preparation of linear alpha-olefins which overcomes the disadvantages of the prior art, especially a method shall be provided which avoids plugging of equipment and piping which are in contact with high molecular weight oligomers containing streams.
- This object is achieved in that a discharge stream of the reactor comprising the solvent, catalyst, linear alpha-olefins and substantially high molecular weight oligomers, the high molecular weight oligomers are separated, then diluted with a dilution medium and heated to about 130°C to about 200°C, the diluted high molecular weight oligomers being then transferred to a disposal device, wherein recycles for loop operation are established, and flow rates of the loop streams are from about 1 to about 50 m3/h.
- Preferably, the high molecular weight oligomers are separated in a separation unit, preferably a filter unit or a distillation unit.
- Preferably, the temperature in the reactor is from about 60 to about 100°C.
- The solvent may be toluene and the dilution medium may be toluene and/or a liquid fraction of the oligomerization product comprising oligomers having more than 18 carbon atoms.
- In one preferred embodiment, the dilution medium comprises the bottom product of a purification apparatus, preferably a distillation column, for the solvent.
- The dilution medium may comprise high molecular weight oligomers.
- The method is further characterized in that the dilution medium with dissolved high molecular weight oligomers is recycled in a loop to increase flow rates from kg/h to m3/h with corresponding stream velocities to avoid plugging of lines.
- Preferably, the disposal device is an incinerator.
- It is also proposed that the high molecular weight oligomers containing streams are agitated.
- Additionally, the dilution ratio of the dilution medium: high molecular weight oligomer may be about 5:1 to about 15:1, preferably about 10:1.
- Finally, according to the invention a reactor system for preparing linear alpha-olefins is provided, especially by an inventive method, comprising a reactor, a separation unit for separating high molecular weight oligomers, recycle loops, and a transfer line to a disposal device.
- Surprisingly, it was found that especially due to the dilution of the high molecular weight oligomers with dilution medium and heating thereof to higher temperatures, plugging of equipment and piping which are in contact with high molecular weight oligomers containing streams can be substantially avoided. Further, no handling of high viscous/solid materials is necessary. Due to the low concentration of the high molecular weight oligomers in the dilution medium, the heat tracing requirements in the inventive method are substantially reduced. Further, the plant availability and reliability in which the oligomerization method is conducted are improved.
- It is obvious that the inventive method is not necessarily restricted to the oligomerization of ethylene to obtain linear alpha-olefins, but may be utilized in all technologies handling high molecular weight oligomers.
- Additional features and advantages of the inventive method are now illustrated in detail with reference to the accompanying drawing wherein
- Fig. 1 shows a schematic illustration of the inventive method for the preparation of linear alpha-olefins.
- In Fig. 1 a reactor 1 for the oligomerization of ethylene to prepare linear alpha-olefins is provided. In the reactor 1 ethylene is oligomerized in the presence of a solvent and a catalyst, preferably at a temperature of about 60-100°C. After oligomerization (the reactor is preferably operated continuously), a discharge stream is removed from the reactor via a
discharge line 2. The discharge stream comprises the solvent, catalyst, liquid linear alpha-olefins and high molecular weight oligomers. The term "high molecular weight oligomers" is meant to comprise oligomers having such a high molecular weight that they are substantially solid at reaction temperature. Additionally, further discharge and feed lines are connected to the reactor, but are omitted for purposes of clarity. The discharge stream may be transferred via thedischarge line 2 to aseparation unit 3, also held at a temperature of about 60-100°C, wherein solid high molecular weight oligomers are separated from the liquid discharge stream. The separation unit may be a filter or any other means suitable and known for someone skilled in the art. Such a separation unit is not absolutely necessary, for example, if no high molecular weight oligomers being solid at reaction temperature are present. The discharge stream containing the substantial amount of solvent and liquid linear alpha-olefins may be processed as is known for someone skilled in the art, for example by distillation of the respective linear alpha-olefins. - The solvent utilized for the oligomerization process is preferably toluene. Toluene is provided to and removed from the reactor by a
reactor flushing system 4. Thereactor flushing system 4 is further connected to a solvent purification apparatus 5, preferably a distillation equipment. In the solvent purification apparatus 5, the solvent may be purified and purified solvent may be reintroduced into the reactor 1. Impurities which may be incorporated in the solvent may be also high molecular weight oligomers which are collected in the bottoms product of the solvent purification apparatus 5. The bottom product may be used as dilution medium. - Separated high molecular weight oligomers are passed via
line 6. Additionally, the bottom product comprising also high molecular weight oligomers is removed from the solvent purification apparatus 5 vialine 7. 6 and 7 are combined. The combined streams are then heated to a temperature of about 130°C to about 200°C so that the high molecular weight oligomers may be diluted or melted (as polyethylene being a major component of the high molecular weight oligomers has a melting point of about 130°C). Preferably, the weight ratio of high molecular weight oligomers and dilution medium is from about 1:5 to about 1:15, preferably 1:10. In a preferred embodiment, the high molecular weight oligomers containing streams are also agitated. The combined streams may be then transferred via line 8 to a tank 9 where the combined streams may be additionally diluted with further dilution medium. Also, fractions of the linear alpha-olefins having more than 18 carbon atoms may be added at this stage, or even earlier or later. As it is still difficult to find economically attractive applications for the fractions of C20+ these fractions may be preferably utilized to dilute the high molecular weight oligomers for disposal. From the tank 9 the diluted high molecular weight oligomers may be then transferred via line 10 to a disposal device, preferably an incinerator 11. From line 10 the diluted high molecular weight oligomers may be also recycled viaLines recycle line 12 into tank 9. The effluent of tank 9 may be also recycled viarecycle line 13 to 6 and 7.lines - Utilizing the inventive method, high molecular weight oligomers containing streams are diluted with an appropriate dilution medium, kept at elevated temperature and, optionally, agitated. In the inventive method, stream velocities in the equipment and piping may be kept high by establishing of larger pump flow rates which are in the range of about 1 to about 50 m3/h. Due to the high stream velocities any plugging of equipment and piping may be avoided. Additionally, the viscosity and pressure drop of the piping system can be adjusted by the dilution rate of the high molecular weight oligomers in the dilution medium. Thus, the small amounts of high molecular weight oligomers (in the range of some kg/h) obtained in the inventive method may be easily disposed by dilution and heating with prevention of plugging.
- The features disclosed in the foregoing description, in the drawing or in the claims may, both separately and in any combination thereof, be material for realizing the invention in diverse forms thereof.
Claims (12)
- Method for the preparation of linear alpha-olefins by oligomerization of ethylene in a reactor in the presence of a solvent and a catalyst, characterized in that from a discharge stream of the reactor comprising the solvent, catalyst, linear alpha-olefins and substantially high molecular weight oligomers, the high molecular weight oligomers are separated, then diluted with a dilution medium and heated to about 130°C to about 200°C, the diluted high molecular weight oligomers being then transferred to a disposal device, wherein recycles for loop operation are established, and flow rates of the loop streams are from about 1 to about 50 m3/h.
- Method according to claim 1, wherein the high molecular weight oligomers are separated in a separation unit, preferably a filter unit or a distillation unit.
- Method according to claim 1, wherein the temperature in the reactor is from about 60 to about 100°C.
- Method according to any of the preceding claims, wherein the solvent is toluene.
- Method according to any of the preceding claims, wherein the dilution medium is toluene and/or a liquid fraction of the oligomerization product comprising oligomers having more than 18 carbon atoms.
- Method according to any of the preceding claims, wherein the dilution medium comprises the bottom product of a purification apparatus, preferably a distillation column, for the solvent.
- Method according to any of the preceding claims, wherein the dilution medium comprises high molecular weight oligomers.
- Method according to any of the preceding claims, wherein the dilution medium with dissolved high molecular weight oligomers is recycled in a loop.
- Method according to any of the preceding claims, wherein the disposal device is an incinerator.
- Method according to any of the preceding claims, wherein the high molecular weight oligomers containing streams are agitated.
- Method according to any of the preceding claims, wherein the dilution ratio of the dilution medium: high molecular weight oligomer is about 5:1 to about 15:1, preferably about 10:1.
- Reactor system for preparing linear alpha-olefins, especially by a method according to any of the claims 1 to 11, comprising a reactor, a separation unit for separating high molecular weight oligomers, recycle loops, and a transfer line to a disposal device.
Priority Applications (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP05016524A EP1749808B1 (en) | 2005-07-29 | 2005-07-29 | Method for the preparation of linear alpha-olefins and reactor system therefore with improved disposal of high molecular weight oligomers |
| DE602005019234T DE602005019234D1 (en) | 2005-07-29 | 2005-07-29 | Process for the preparation of linear alpha olefins and reactor system therefor with disposal of high molecular weight oligomers |
| PCT/EP2006/005641 WO2007016992A1 (en) | 2005-07-29 | 2006-06-13 | Method for the preparation of linear alpha-olefins and reactor system therefor with disposal of high molecular weight oligomers |
| CN2006800279278A CN101238086B (en) | 2005-07-29 | 2006-06-13 | Process for producing linear alpha-olefins and reactor system therefor including high molecular weight oligomer treatment |
| JP2008523146A JP5060477B2 (en) | 2005-07-29 | 2006-06-13 | Process for the preparation of linear alpha olefins with improved disposal of high molecular weight oligomers and reactor system therefor |
| ZA200800832A ZA200800832B (en) | 2005-07-29 | 2006-06-13 | Method for the preparation of linear alpha-olefins and reactor system therefor with disposal of high molecular weight oligomers |
| RU2008107708/04A RU2406716C2 (en) | 2005-07-29 | 2006-06-13 | Method of producing linear alpha-olefins with improved removal of high molecular weight oligomers and reactor system for realising said method |
| US11/989,831 US7723557B2 (en) | 2005-07-29 | 2006-06-13 | Method for the preparation of linear alpha-olefins and reactor system therefore with improved disposal of high molecular weight oligomers |
| MYPI20062813A MY140788A (en) | 2005-07-29 | 2006-06-14 | Method for the preparation of linear alpha-olefins and reactor system therefor with improved disposal of high molecular weight oligomers |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP05016524A EP1749808B1 (en) | 2005-07-29 | 2005-07-29 | Method for the preparation of linear alpha-olefins and reactor system therefore with improved disposal of high molecular weight oligomers |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP1749808A1 true EP1749808A1 (en) | 2007-02-07 |
| EP1749808B1 EP1749808B1 (en) | 2010-02-03 |
Family
ID=35517552
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP05016524A Ceased EP1749808B1 (en) | 2005-07-29 | 2005-07-29 | Method for the preparation of linear alpha-olefins and reactor system therefore with improved disposal of high molecular weight oligomers |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US7723557B2 (en) |
| EP (1) | EP1749808B1 (en) |
| JP (1) | JP5060477B2 (en) |
| CN (1) | CN101238086B (en) |
| DE (1) | DE602005019234D1 (en) |
| MY (1) | MY140788A (en) |
| RU (1) | RU2406716C2 (en) |
| WO (1) | WO2007016992A1 (en) |
| ZA (1) | ZA200800832B (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2017109725A1 (en) * | 2015-12-22 | 2017-06-29 | Sabic Global Technologies B.V. | Methods for toluene recovery from linear alpha olefin production |
| WO2023036767A1 (en) * | 2021-09-08 | 2023-03-16 | Sabic Global Technologies B.V. | Method for flushing reactor |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109134275B (en) * | 2012-05-04 | 2026-04-21 | 科思创德国股份有限公司 | Methods for treating mixtures of substances containing aromatic amines, particularly mixtures of crude aniline. |
| US20190322965A1 (en) * | 2015-12-04 | 2019-10-24 | Sabic Global Technologies B.V. | Process for flushing an oligomerization reactor and oligomerization of an olefin |
| CN108778479A (en) * | 2016-03-21 | 2018-11-09 | 沙特基础工业全球技术有限公司 | Method for handling oligomerization product stream |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5496783A (en) * | 1992-07-09 | 1996-03-05 | Institut Francais Du Petrole | Catalyst for the production of light alpha olefins by oligomerization of ethylene |
| US5817905A (en) * | 1996-04-26 | 1998-10-06 | Institut Francais Du Petrole | Process for the conversion of ethylene into light alpha olefins with the use of additives based on quaternary ammonium salts |
| US6221986B1 (en) * | 1997-02-25 | 2001-04-24 | Institut Francais Du Petrole | Process for converting ethylene to light alpha olefins |
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| US4547612A (en) * | 1984-09-25 | 1985-10-15 | Mobil Oil Corporation | Production of lubricant and/or heavy distillate range hydrocarbons by light olefin upgrading |
| JPS6140307A (en) * | 1984-08-01 | 1986-02-26 | Mitsui Toatsu Chem Inc | Method of recovering diluent |
| US4891457A (en) * | 1985-09-13 | 1990-01-02 | Hartley Owen | Multistage process for converting olefins to heavier hydrocarbons |
| DE3844180A1 (en) * | 1988-12-29 | 1990-07-05 | Hoechst Ag | METHOD FOR SEPARATING VOLATILE COMPONENTS FROM REACTION MIXTURES OBTAINED BY HIGH PRESSURE POLYMERIZATION |
| SU1820601A1 (en) * | 1989-05-26 | 1995-10-27 | Институт нефтехимических процессов им.Ю.Г.Мамедалиева | METHOD OF SYNTHESIS OF LINEAR α-OLEFINS C-C |
| JP3486212B2 (en) * | 1993-10-26 | 2004-01-13 | 三菱化学株式会社 | Method for producing low α-olefin polymer |
| US5523508A (en) * | 1994-12-29 | 1996-06-04 | Uop | Process for linear alpha-olefin production: eliminating wax precipitation |
| JPH08283330A (en) * | 1995-04-18 | 1996-10-29 | Mitsubishi Chem Corp | Process for producing α-olefin low polymer |
| US5811608A (en) * | 1995-12-15 | 1998-09-22 | Uop Llc | Process for oligomer production and saturation |
| JP3549136B2 (en) * | 1996-07-30 | 2004-08-04 | 三菱化学株式会社 | Method for producing low α-olefin polymer |
| JP2002256007A (en) * | 2000-12-26 | 2002-09-11 | Idemitsu Petrochem Co Ltd | METHOD FOR PRODUCING alpha-OLEFIN OLIGOMER |
| JP3904530B2 (en) * | 2003-04-07 | 2007-04-11 | 三菱化学株式会社 | Method for producing α-olefin low polymer |
-
2005
- 2005-07-29 DE DE602005019234T patent/DE602005019234D1/en not_active Expired - Lifetime
- 2005-07-29 EP EP05016524A patent/EP1749808B1/en not_active Ceased
-
2006
- 2006-06-13 CN CN2006800279278A patent/CN101238086B/en not_active Expired - Fee Related
- 2006-06-13 RU RU2008107708/04A patent/RU2406716C2/en active
- 2006-06-13 JP JP2008523146A patent/JP5060477B2/en not_active Expired - Fee Related
- 2006-06-13 WO PCT/EP2006/005641 patent/WO2007016992A1/en not_active Ceased
- 2006-06-13 US US11/989,831 patent/US7723557B2/en not_active Expired - Fee Related
- 2006-06-13 ZA ZA200800832A patent/ZA200800832B/en unknown
- 2006-06-14 MY MYPI20062813A patent/MY140788A/en unknown
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5496783A (en) * | 1992-07-09 | 1996-03-05 | Institut Francais Du Petrole | Catalyst for the production of light alpha olefins by oligomerization of ethylene |
| US5817905A (en) * | 1996-04-26 | 1998-10-06 | Institut Francais Du Petrole | Process for the conversion of ethylene into light alpha olefins with the use of additives based on quaternary ammonium salts |
| US6221986B1 (en) * | 1997-02-25 | 2001-04-24 | Institut Francais Du Petrole | Process for converting ethylene to light alpha olefins |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2017109725A1 (en) * | 2015-12-22 | 2017-06-29 | Sabic Global Technologies B.V. | Methods for toluene recovery from linear alpha olefin production |
| US10781147B2 (en) | 2015-12-22 | 2020-09-22 | Sabic Global Technologies B.V. | Methods for toluene recovery from linear alpha olefin production |
| WO2023036767A1 (en) * | 2021-09-08 | 2023-03-16 | Sabic Global Technologies B.V. | Method for flushing reactor |
| US12465961B2 (en) | 2021-09-08 | 2025-11-11 | Sabic Global Technologies B.V. | Method for flushing reactor |
Also Published As
| Publication number | Publication date |
|---|---|
| CN101238086A (en) | 2008-08-06 |
| MY140788A (en) | 2010-01-15 |
| JP2009503154A (en) | 2009-01-29 |
| WO2007016992A1 (en) | 2007-02-15 |
| RU2008107708A (en) | 2009-09-10 |
| DE602005019234D1 (en) | 2010-03-25 |
| EP1749808B1 (en) | 2010-02-03 |
| US20090221769A1 (en) | 2009-09-03 |
| US7723557B2 (en) | 2010-05-25 |
| RU2406716C2 (en) | 2010-12-20 |
| ZA200800832B (en) | 2009-05-27 |
| JP5060477B2 (en) | 2012-10-31 |
| CN101238086B (en) | 2012-06-20 |
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